Refine
Has Fulltext
- yes (322)
Is part of the Bibliography
- yes (322)
Year of publication
- 2024 (4)
- 2023 (9)
- 2022 (29)
- 2021 (37)
- 2020 (29)
- 2019 (19)
- 2018 (8)
- 2017 (4)
- 2016 (15)
- 2015 (3)
- 2014 (2)
- 2013 (3)
- 2012 (3)
- 2011 (2)
- 2010 (2)
- 1994 (20)
- 1993 (9)
- 1992 (10)
- 1991 (9)
- 1990 (11)
- 1989 (10)
- 1988 (10)
- 1987 (9)
- 1986 (11)
- 1985 (6)
- 1984 (3)
- 1983 (6)
- 1982 (4)
- 1981 (3)
- 1980 (3)
- 1979 (4)
- 1978 (4)
- 1977 (1)
- 1976 (1)
- 1975 (4)
- 1974 (1)
- 1973 (8)
- 1972 (3)
- 1971 (1)
- 1968 (1)
- 1967 (1)
Document Type
- Journal article (322) (remove)
Keywords
- Organische Chemie (122)
- fluorescence (10)
- Chemie (9)
- self-assembly (9)
- water oxidation (9)
- 1 (8)
- 3 (7)
- RNA (7)
- photocatalysis (7)
- polycyclic aromatic hydrocarbons (7)
- organic chemistry (6)
- Diels-Alder reactions (5)
- SARS-CoV-2 (5)
- dyes (5)
- liquid crystals (5)
- luminescence (5)
- chemistry (4)
- circular dichroism (4)
- dyes/pigments (4)
- in vitro selection (4)
- perylene bisimide (4)
- sphingolipids (4)
- structure elucidation (4)
- supramolecular chemistry (4)
- 4-0xadiazin-6-ones (3)
- absolute configuration (3)
- aggregation (3)
- aromaticity (3)
- artificial photosynthesis (3)
- boranes (3)
- catalysis (3)
- cell imaging (3)
- ceramide (3)
- ceramides (3)
- chirality (3)
- energy transfer (3)
- exciton coupling (3)
- homogeneous catalysis (3)
- kinetics (3)
- macrocycles (3)
- molecular docking (3)
- organic photodiodes (3)
- photoinduced electron transfer (3)
- 2 (2)
- 4-0xadiazine-2-carboxylate (2)
- 6 (2)
- Anorganische Chemie (2)
- Carbocations (2)
- Chili RNA Aptamer (2)
- Deoxyribozymes (2)
- Design (2)
- Dyes (2)
- Enol Iactones (2)
- Epitranscriptomics (2)
- Fluorescence (2)
- G-quadruplexes (2)
- Holothuria spinifera (2)
- J‐aggregates (2)
- Ketenes (2)
- LC-HRESIMS (2)
- RNA modification (2)
- RNA-dependent RNA polymerase (2)
- Ruthenium complexes (2)
- UV/Vis spectroscopy (2)
- X-ray crystallography (2)
- absorption (2)
- acid sphingomyelinase (2)
- annulation (2)
- azulene (2)
- boronate esters (2)
- cage compounds (2)
- cerebrosides (2)
- chirality transfer (2)
- click chemistry (2)
- corannulene (2)
- covalent organic frameworks (2)
- crystal engineering (2)
- cyclophanes (2)
- cytotoxic activity (2)
- cytotoxicity (2)
- density functional calculations (2)
- diketopyrrolopyrroles (2)
- dynamic covalent chemistry (2)
- electrocatalysis (2)
- fullerenes (2)
- helicenes (2)
- heterogeneous catalysis (2)
- hexahydro- (2)
- homogenous catalysis (2)
- hydrocarbons (2)
- hydrogen bonding (2)
- ligands (2)
- lysosome (2)
- marine natural product (2)
- merocyanines (2)
- methyl 6-oxo-5-phenyl- (2)
- nanographene (2)
- optical spectroscopy (2)
- organic semiconductors (2)
- organic solar cells (2)
- pentacene (2)
- perylene bisimides (2)
- phosphorescence (2)
- polymerization (2)
- polymers (2)
- porphyrins (2)
- preparation (2)
- renewable fuels (2)
- ribozymes (2)
- ruthenium (2)
- ruthenium bda complexes (2)
- ruthenium complexes (2)
- singlet oxygen (2)
- site-specific RNA cleavage (2)
- solid-state emitters (2)
- solvent effects (2)
- spectroscopy (2)
- squaraine dyes (2)
- stereochemistry (2)
- streptomyces (2)
- supramolecular polymers (2)
- thermodynamics (2)
- two-photon absorption (2)
- two-photon excited fluorescence (2)
- water (2)
- water splitting (2)
- y-oxo- (2)
- 0]hexane (1)
- 1' -c]naphthalene (1)
- 1-aryl- (1)
- 1-dibromo-1a (1)
- 10 (1)
- 11-dihydro- / 1-Pyrazoline (1)
- 2-Bismethylenecyclobutanes (1)
- 2-Bismethylenecyclohexane (1)
- 2-Cyclopentanedione derivatives (1)
- 2-Norcaranols (1)
- 2-photon absorption (1)
- 2-α:2' (1)
- 3-Azabicyclo{3 (1)
- 3-Methenonaphthalenes (1)
- 3-aryl- (1)
- 3-cyclohexadiene (1)
- 3-n-butyl-N-phenyl- (1)
- 4 (1)
- 4-Pentadienylamine (1)
- 4-tetrahydro- (1)
- 4</sup>.0<sup>3 (1)
- 4]0xadiazino[4 (1)
- 4]non-7-en-6-ylpotassium (1)
- 4a (1)
- 5 (1)
- 5-b]isoquinolin-1-one derivatives (1)
- 5-dinitrobenzoates (1)
- 5</sup>]beptanes (1)
- 5H-Dibenzo[a (1)
- 5]cyclohepta[ 1 (1)
- 6-Norpinanols (1)
- 6-Norpinyl 3 (1)
- 6-Thiatricyclo[3.2.1.o 2.7 ]oct-3-ene 6 (1)
- 6-aryl- (1)
- 6-dibromo-3-phenyl- (1)
- 6-dioxide (1)
- 6-phenyl (1)
- 6H-1 (1)
- 6a-Tetrahydro-2H-cyclobuta[b]pyrans (1)
- 7 (1)
- 7-Norcaranylidene carbenoid (1)
- 7-dibromo (1)
- 7</sup>]heptane derivatives (1)
- 7b-tetrahydro- (1)
- 8 (1)
- 8-Tetrahydro-3H-2-benzopyrans (1)
- 8a-Tetrahydro-2H-1-benzopyran (1)
- ADME analysis (1)
- AIE (1)
- API (1)
- Adipic acid (1)
- Aldehyde Bioconjugation (1)
- Alkyltransferase Ribozyme SAMURI (1)
- Allenes (1)
- Alzheimer′s disease (1)
- Amplification (1)
- Anchimeric assistance in solvolysis (1)
- Ancistrocladus ealaensis (1)
- Ancistrocladus likoko (1)
- Antiviral nucleoside analogues (1)
- Apoptosis (1)
- Aromatic-hydrocarbon (1)
- Aspergillus niger (1)
- Atomic and molecular interactions with photons (1)
- Auflösungsraten (1)
- BMP-2 (1)
- BMP-2 delivery (1)
- Bacillus megaterium (1)
- Baltic Sea (1)
- Barbaralane derivatives (1)
- Benzocycloheptene derivatives (1)
- Bicyclo[1.1.0]butane derivatives (1)
- Bicyclo[1.1.0]butanes (1)
- Bicyclo[1.1.0]butylcarbinyl sulfonates (1)
- Bicyclo[2.1.l]hexan-5-one (1)
- Bicyclo[3.2.0.0<sup>2 (1)
- Bicyclo[3.2.0]hept-6-ene derivatives (1)
- Bicyclo[3.2.1]oct-3-en-2-yl anions (1)
- Biochemistry (1)
- Biocompatibility (1)
- Biodegradable polymer scaffolds (1)
- Bioorthogonal Tag (1)
- Bisbenzo[ 4 (1)
- Bone morphogenetic protein-2 (1)
- Bone tissue engineering (1)
- Butadien (1)
- C-13 NMR (1)
- C-C coupling (1)
- CCL2 (MCP-1) (1)
- CD4+ T cells (1)
- CD8+ T cells (1)
- CXCL8 (IL-8) (1)
- Caco-2 (1)
- Carbene insertion (1)
- Carbon (1)
- Ceramide (1)
- Chemical modification (1)
- Chiralität (1)
- Chromophore Assembly (1)
- Chromophores (1)
- Co-Crystal Structures of Chili RNA (1)
- Conjugated polymers (1)
- Corannulene (1)
- Cryoelectron Microscopy (1)
- Cryoelectron microscopy (1)
- Cycloadditions (1)
- Cycloallene dimerization (1)
- Cyclobuta[c}pyridines (1)
- Cyclobutylcarbinyl sulfonates (1)
- Cyclohept-3-en-1-ols (1)
- Cyclopropanetetracarbonitrile derivatives (1)
- DNA (1)
- DNA catalysis (1)
- DNA/RNA binding (1)
- DNA/RNA sensors (1)
- DNS-Schädigung (1)
- Deoxyribozyme (1)
- Dictyota (1)
- Dictyotaceae (1)
- Dimers (1)
- Donor−acceptor dyads (1)
- EPR (1)
- Effectors in plant pathology (1)
- Electron (1)
- Electron demand in ditosylates (1)
- Electron transfer (1)
- Emission (1)
- Energy transfer (1)
- Enzymes (1)
- Eriodictyon californicum (1)
- FT-IR spectroscopy (1)
- Festkörper-NMR (1)
- Fiels-effect transistors (1)
- Fluorescence and Crosslinking (1)
- Fluoreszenz (1)
- Fluoreszenzresonanz-Energietransfer (1)
- Fluorogenic RNA Aptamers (1)
- Functional nucleic acids (1)
- Functionalization (1)
- Fungal host response (1)
- Garcinia biflavonoids (1)
- Gibbs activation energy (1)
- Glycosyltransferase (1)
- Golgi (1)
- Graphene nanoribbons (1)
- Growth; BMP-2 (1)
- H2A histone family member X (H2AX) (1)
- HIV (1)
- HRMS (1)
- Halonium ions (1)
- Helicen (1)
- High efficiency (1)
- High performance (1)
- Homo Diels-Alder reactions (1)
- Homoaromaticity in carbanions (1)
- Homobenzvalene (1)
- Hyperfine coupling constants (1)
- In-vitro (1)
- Indirect and direct contributions to A<sub>iso</sub> (1)
- Influence of excitation classes (1)
- Intensity (1)
- Isomorphe Nukleobasen-Analoga (1)
- Isoquinolines (1)
- J-aggregate behavior (1)
- J-aggregates (1)
- Jurkat cells (1)
- K-region (1)
- K2–K model (1)
- Koordinationsisomerie (1)
- Lactone conformations (1)
- Lectins (1)
- Light-emitting diodes (1)
- Line-shape analysis (1)
- Lippert–Mataga plot (1)
- Liquid-crystalline (1)
- Long-range coupling constants (1)
- MAS (1)
- METTL8 (1)
- Mandibular continuity defects (1)
- Marcus inverted region (1)
- Marrow stromal cells (1)
- Merocyanine (1)
- Mesenchymal transition (1)
- Microenvironment (1)
- Migratory aptitudes in carbocations (1)
- Mitochondrial Matrix Protein (1)
- Mizellen (1)
- Modified Nucleotides in tRNAs (1)
- Molecular mechanism (1)
- Molecular-dynamics (1)
- Molecules (1)
- Molnupiravir (1)
- Molnupiravir-Induced RNA Mutagenesis Mechanism (1)
- Multibranched structures (1)
- N-oleoyl serinol (1)
- NDI-H (1)
- NIR OLED (1)
- NMR spectroscopy (1)
- Nahordnung (1)
- Naphthylisoindolinone alkaloids (1)
- Neighbouring group participation (1)
- Neisseria (1)
- Nonbonded Interactions (1)
- Norcaranes (1)
- Norpinanes (1)
- Nucleic Acids (1)
- Nucleobase Analogue (1)
- OEG chains (1)
- Octavalen (1)
- Oligofructoside (1)
- One-photon (1)
- Optical Spectroscopy (1)
- Optical properties (1)
- Optical spectroscopy (1)
- Oral squamous cell carcinoma (1)
- Organelles (1)
- Organobor (1)
- PBI cyclophane (1)
- PI stacking (1)
- Pathway (1)
- Perovskite (1)
- Phaeophyceae (1)
- Photochemistry (1)
- Photoelektron (1)
- Photoresponsives Verhalten (1)
- Polymer-drug interaction (1)
- Polymere (1)
- Polymers (1)
- Potential-energy curves (1)
- QM/MM (1)
- RNA Enzymes (1)
- RNA Labelling (1)
- RNA Methyltransferase (1)
- RNA Modification (1)
- RNA aptamers (1)
- RNA labeling (1)
- RNA ligation (1)
- RNA splicing (1)
- RNA-Aptamere (1)
- RNA-Dependent RNA Polymerase (1)
- RU-(II) complexes (1)
- Radical-ion pair (1)
- Rearrangement of carbocations (1)
- Remdesivir (1)
- Ribozyme (1)
- Ru(II)–Fe(II)–Ru(II) complex (1)
- SARS-CoV-2 polymerase (1)
- SARS-CoV2 Replication Impairment (1)
- SacB (1)
- Scleractinia (1)
- Screening (1)
- Selbstassemblierung (1)
- Simulations (1)
- Sinus floor augmentation (1)
- Site-Specific RNA Cleavage (1)
- Site-specific RNA labelling (1)
- Solution-state NMR (1)
- Spin density (1)
- Spirotetracyclo[4.1.0.0<sup>2 (1)
- Squamous-cell carcinoma (1)
- Sracking (1)
- Staphylococcus aureus (1)
- State (1)
- Stereochemistry (1)
- Stokes-Verschiebung (1)
- Stokes-shifted fluorescence emission (1)
- Streptomyces axinellae (1)
- Structural Biology (1)
- Structure elucidation (1)
- Struktursonden (1)
- Stylissa carteri (1)
- Suc1 (1)
- Supramolecular Element (1)
- Supramolekulare Polymere (1)
- Suzuki coupling (1)
- Synthetic Functional RNAs (1)
- Systems (1)
- TERRA RNA (1)
- Tetrakis(arylmethylene)ethane diradical (1)
- Thalassodendron ciliatum (1)
- Tricyclo[3.3.1.0 2 (1)
- Tricyclo[4.1.0.0<sup>2.7</sup>]heptanes (1)
- Tumorigenicity (1)
- Urazoles (1)
- Vibronic contributions (1)
- X-ray Crystallography (1)
- X-ray diffraction (1)
- XNA (1)
- XRPD (1)
- Zirkulardichroismus (1)
- [1 (1)
- [2 + 2]- and [4 + 2]- (1)
- [n]helicenes (1)
- \(\alpha\)-phase (1)
- \(\beta\)-phase (1)
- \(^{1}\)H-\(^{13}\)C HETCOR (1)
- abietane (1)
- activating transcription factor 4 (ATF4) (1)
- adsorption (1)
- aelf-assembly (1)
- alkaloids (1)
- alpha (1)
- amphiphilic dyes (1)
- amplification (1)
- ancistrocladinium A (1)
- annihilation (1)
- anti-cancer-agent (1)
- anti-depressant drug (1)
- anti-trypanosomal (1)
- antibacterial activity (1)
- antidepressants (1)
- antimicrobials (1)
- aqua material (1)
- aqueous medium (1)
- arene-fluoroarene (1)
- arenes (1)
- aromatic compounds (1)
- artificial base pair (1)
- association (1)
- ataxia teleagiectasia mutated (ATM) (1)
- azaborole (1)
- azaphilone (1)
- azido-ceramides (1)
- bacterial infection (1)
- bartalinia robillardoides (1)
- bicyclic (1)
- biflavanoids (1)
- bile salt (1)
- bioactive compound (1)
- bioactivities (1)
- biocatalysis (1)
- biocompatibility (1)
- biological techniques (1)
- biomass (1)
- bioorthogonal SAM analogue ProSeDMA (1)
- bioorthogonal metabolic glycoengineering; click chemistry; sialic acid (1)
- biophysical investigation (1)
- biosynthesis (1)
- bis-terpyridyl ligands (1)
- boric acid (1)
- boron (1)
- boronateesters (1)
- borylation (1)
- brown seaweeds (1)
- bulk-heterojunction solar cells (1)
- carbon (1)
- carrier transport (1)
- cascade reactions (1)
- catalyst (1)
- catalyst synthesis (1)
- catalysts (1)
- catalytic (1)
- catalytic activity (1)
- catalytic mechanisms (1)
- cell membrane model (1)
- cellular stress response (1)
- ceramidase (1)
- ceramide analogs (1)
- cerebroside (1)
- ceriops decandra (1)
- charge transport (1)
- charge transport; hydrogen bonding; oligothiophene; organogel; self-assembly (1)
- chemical modification (1)
- chiral resolution (1)
- circular polarized luminescence (1)
- circularly polarized luminescence (1)
- classical and nonclassical (1)
- co-aggregation (1)
- cocrystallization (1)
- colloid (1)
- columnar phases (1)
- complexation (1)
- complexity (1)
- configurational stability (1)
- conformation (1)
- conjugated molecule (1)
- cooperative self-assembly (1)
- coordination chemistry (1)
- coordination isomerism (1)
- coordination oligomer (1)
- coordination oligomers (1)
- covalent organic framework (1)
- cristal engeneering (1)
- crystalline (1)
- crystals (1)
- curcumin (1)
- curvature (1)
- curved π-systems (1)
- cyclic / 1-0xa-2 (1)
- cyclic perylene bisimide (1)
- cyclodehydrogenation (1)
- cylindrical micelles (1)
- cysteine protease (1)
- cytoplasm (1)
- d]cycloheptene (1)
- decandrinin (1)
- deoxyribozymes (1)
- deracemization (1)
- di-\(\pi\)-methane rearrangement (1)
- dibenzosemibullvalenes (1)
- differential scanning calorimetry (1)
- diffusion (1)
- dimerization (1)
- dimers (1)
- dinuclear (1)
- dipole-dipole interaction (1)
- discotic liquid crystals (1)
- discovery (1)
- dissolution rates (1)
- disulfide bonds (1)
- docking (1)
- docking studies (1)
- donor-acceptor dyad (1)
- donor-acceptor interactions (1)
- donor–acceptor (1)
- donor–acceptor dyads (1)
- drug delivery (1)
- drugs (1)
- duplex structure (1)
- dye assembly (1)
- dye chemistry (1)
- electrodes (1)
- electronic and spintronic devices (1)
- electronic collective variables (1)
- electronic devices (1)
- electronic structure (1)
- electronic wavefunction (1)
- emission (1)
- enantiomerization (1)
- enantiomers (1)
- encapsulation (1)
- enzyme (1)
- enzyme purification (1)
- enzyme structure (1)
- enzymes (1)
- epitranscriptomics (1)
- ergosterol derivative (1)
- ethenoanthracenes (1)
- excimer (1)
- excimer formation (1)
- extractives (1)
- ferroelectrics (1)
- films (1)
- flavenoids (1)
- flavonoids (1)
- flourescence quantum yield (1)
- fluerescence (1)
- fluorenscence (1)
- fluorescence resonance energy transfer (1)
- fluorescence spectroscopy (1)
- fluorescent (1)
- fluorescent probes (1)
- fluorogen-activating RNA aptamer (FLAP) (1)
- fluoxetine (1)
- flux (1)
- folded macrocyles (1)
- folding (1)
- folding landscapes (1)
- functionalization (1)
- generation and rearrangement (1)
- glycocalyx (1)
- glycosphingolipids (1)
- growth (1)
- guttiferae (1)
- hMSC-TERT (1)
- halichondria panicea (1)
- heavy metals (1)
- helicene (1)
- heterocycles (1)
- hexakisadducts (1)
- high-temperature NMR (1)
- highly substituted (1)
- homochiral dimer (1)
- host-guest systems (1)
- hybrid materials (1)
- hydrazone (1)
- hydrogen peroxide (1)
- hydrolysis (1)
- hydroxylation (1)
- imaging (1)
- imidization (1)
- imines (1)
- in vitro Selection (1)
- induced phase transition (1)
- inflammation (1)
- intersystem crossing (1)
- intrinsic free space (1)
- invasion (1)
- inflammatory response (1)
- ion pairing (1)
- iron oxide nanoparticles (1)
- isomorphic nucleobase analog (1)
- key structure - fluorescence activation relationships (SFARs) (1)
- kinetics of thermolysis (1)
- lH-Cyclopropa[a]naphthalenes (1)
- large stokes shift (1)
- laser (1)
- lectin (1)
- ligand binding (1)
- liposome (1)
- liquid crystal alignment (1)
- livingstonei (1)
- luminescent solar concentrators (1)
- macrocycle (1)
- major depression (1)
- marine bacteria (1)
- marine fungi (1)
- marine macroalgae (1)
- marine natural products (1)
- marine sponge (1)
- materials (1)
- materials design (1)
- measles (1)
- mechanism (1)
- merocyanine (1)
- merocyanine dyes/pigments (1)
- mesogens (1)
- metabolic analysis (1)
- metabolic glycoengineering (1)
- metadynamics (1)
- metal complexenes (1)
- metal-to-ligand charge transfer (MLCT) (1)
- metallomacrocycles (1)
- methyl viologen (1)
- methyltransferase (1)
- micelles (1)
- microbiology (1)
- microbiology techniques (1)
- microscopy (1)
- microtubes (1)
- migration (1)
- minimal inhibitory concentration (1)
- mobility (1)
- modified monosaccharides (1)
- molecular (1)
- molecular capsules (1)
- molecular dynamics (1)
- molecules (1)
- mtrogen extruston (1)
- multiflora (1)
- multimetallic complexes (1)
- multiple myeloma (1)
- nanoparticles (1)
- nanorods and nanosheets (1)
- nanoscale imaging (1)
- nanosegregation (1)
- nanotube (1)
- naphthalene diimide (1)
- naphthylisoquinoline alkaloid (1)
- naphthylisoquinoline alkaloids (1)
- narrow bandwidth (1)
- natural products (1)
- near infrared emitter (1)
- near-infrared sensitivity (1)
- non-fullerene acceptors (1)
- noncovalent interactions (1)
- nonfullerene acceptors (1)
- nucleation elongation (1)
- nucleation-elongation (1)
- nucleation-elongation model (1)
- nucleic acids (1)
- nucleoside modification recognition (1)
- obstructive pulmonary disease (1)
- oligomers (1)
- oligothiophene (1)
- oligothiophenes (1)
- optical materials (1)
- optics (1)
- organic semiconductors (1)
- organic compounds (1)
- organic light emitting diodes (1)
- organization (1)
- orylation (1)
- oxidation (1)
- oxygen reduction reaction (1)
- p-conjugated systems (1)
- pancreatic cancer (1)
- parallel polar dimers (1)
- pentaketide (1)
- peptide backbone (1)
- perylene (1)
- perylene bisimide dyes (1)
- perylene bisimide hydrogels (1)
- perylene bismide dye (1)
- perylene dyes (1)
- perylene imide (1)
- perylenebisimide (1)
- perylenebisimide dyes (1)
- phenazine (1)
- phenyl-substituted (1)
- phenylboronate (1)
- phosphodiesterase-4 inhibitor (1)
- photochemical (1)
- photoconductive interlayer (1)
- photoluminescence (1)
- photoresponsive behavior (1)
- photosenitizers (1)
- photosensitization (1)
- phthalocyanines (1)
- platinum complexes (1)
- pol(2-oxazoline) (1)
- polarizing optical microscopy (1)
- poly(2-oxazine) (1)
- polycycles (1)
- polycyclic (1)
- polycyclic aromatic hydrocarbon (1)
- polymer drug interaction (1)
- polymorphism (1)
- polyoxazolines (1)
- polypyridyl complexes (1)
- porous materials (1)
- porousmaterials (1)
- probes (1)
- protease inhibition (1)
- proteasome inhibitor resistance (1)
- proteasome subunit beta type-5 (PSMB5) (1)
- push–pull thienylthiazole (1)
- pyrene (1)
- quantum chemical analysis (1)
- quantum optics (1)
- racemization (1)
- radical (1)
- radical anion (1)
- reabsorption (1)
- real-time NMR spectroscopy (1)
- rearrangement (1)
- recombinant proteins (1)
- redox (1)
- regulatory T cells (1)
- regulatory T cells (Treg) (1)
- renew-able fuels (1)
- rhizophoraceae (1)
- rigidification (1)
- rofumilast (1)
- room-temperature phosphorescence (RTP) (1)
- rotational diffusion (1)
- ruthenium catalysts (1)
- sSupramolecular interaction (1)
- scanning probe microscopy (1)
- seagrass (1)
- self-sorting (1)
- separation techniques (1)
- shape-amphiphiles (1)
- short-range order (1)
- sialic acids (1)
- simulated intestinal fluid (1)
- single crystal structure (1)
- site-specific RNA labeling (1)
- six-membered (1)
- social self‐sorting (1)
- solar cells (1)
- solar fuels (1)
- solid-state NMR (1)
- solid-state NMR spectroscopy (1)
- solid‐state emission (1)
- solubility (1)
- solvatochromism (1)
- solvolysis of (1)
- spectroscopic analysis (1)
- sphingolipid expansion microscopy (1)
- sphingomyelinase (1)
- sphingosine (1)
- sphingosine 1-phosphate (1)
- sphingosine kinases (1)
- stability (1)
- star-shaped compounds (1)
- starazine (1)
- starphene analogue (1)
- stereospecific sythesis (1)
- sterubin (1)
- stokes shift (1)
- structural biology (1)
- structural changes (1)
- structural dynamics (1)
- structure probes (1)
- structure probing (1)
- structure–function relation (1)
- structure–property relation (1)
- subphthalocyanine (1)
- substituted (1)
- substituted 2-oxo- dimethyl esters (1)
- superparamagnetism (1)
- superstructure (1)
- supramolecular assembly (1)
- supramolecular folding (1)
- supramolecular materials (1)
- supramolecular polymerization (1)
- surface interactions (1)
- survival (1)
- sustainable energy source (1)
- swallow-tail (1)
- systems (1)
- template catalysis (1)
- tenofovir (1)
- tethya aurantium (1)
- tetracoordinated boron (1)
- tetromycin (1)
- theranostics (1)
- thin-film transistors (1)
- time-resolved impulsive stimulated raman spectroscopy (1)
- tissue engineering (1)
- transient absorption (1)
- triarylamine (1)
- triarylborane (1)
- trinuclear (1)
- triplet (1)
- triplet sensitization (1)
- two-dimensional nanostructures (1)
- umbrella-shaped mesogens (1)
- upconversion (1)
- upramolecular polymerization process (1)
- vacuum processable (1)
- vibrational coherence (1)
- viral epidemiology (1)
- viral infection (1)
- water oxidation catalysis (1)
- y-Oxoketenes (1)
- zooxanthellae (1)
- ß-Lactones (1)
- ß-unsaturated (1)
- β-Lactones (1)
- δ-Lactones (1)
- δ-chloro- (1)
- π-Konjugierte Systeme (1)
- π-conjugated systems (1)
- π-extension (1)
- π-π-interactions (1)
- π–π Stacking (1)
Institute
- Institut für Organische Chemie (322) (remove)
Sonstige beteiligte Institutionen
- Agricultural Center, BASF SE, 67117 Limburgerhof, Germany (1)
- Cluster of Excellence "Multiscale Bioimaging: from Molecular Machines to Networks of Excitable Cells, Göttingen (1)
- Department of Cellular Biochemistry, University Medical Center Göttingen (1)
- Department of Cellular Biochemistry, University Medical Centre Göttingen (1)
- Department of Molecular Biology, University Medical Centre Göttingen (1)
- Georg August University School of Science (1)
- Göttingen Center for Molecular Biosciences, University of Göttingen (1)
- Helmholtz Institute for RNA-based Infection Biology (HIRI), Josef-Schneider-Straße 2/D15, DE-97080 Wuerzburg, Germany (1)
- Institut für Molekulare Infektionsbiologie (MIB) der Universität Würzburg (1)
- Institute of Cancer Research (ICR) London (1)
The 130 chemical shifts were determined of the carbons in 12 cycloheptanes, 21 cycloheptanols, and 8 cycloheptanones. In some cyc1oheptanols and cyc1oheptanones, the assignments have been obtained unambiguously by the synthesis of deuterated derivatives and the use of paramagnetic-shift reagents. Substituent effects for the different types of groups have been calculated. The most informative data about the cyc10heptane conformations were provided by the relatively well understood I' effects. The results are generally in,good agreement with predictions based on the twist-chair form, which has been predicted by Hendrickson to be the most stable conformation. Pairs of cis-trans isomers are found to have rather characteristic differences in their 130 spectra. This fact was used to assign the resonances found for cis-trans mixtures of methyl-substituted cyc1oheptanols to specific isomers.
No abstract available
No abstract available
By means of the BC NMR spectra of tricyclo{2.2.0~rfJ6Jhexane and thirteen of its derivatives the effects of substituents in endo-3- and endo-5-positions on the HC chemical shifts have been determined. The y-anti effects are at least as Jarge as in monosubstituted cyc1obutanes, where the shielding values of second-row hetero substituents exceed those in unstrained systems by far, and higher-row and carbon substituents still cause substantial upfield shifts. In the title system the y-anti effect of a substituent in the endo-3- and endo-5-position are operative additively, and thus shift the absorption of C-J upfieJd by a maximum of 27 ppm with respect to the unsubstituted hydrocarbon.
No abstract available
7-Azatetracyclo[4.1.0.0<sup>2,4</sup>.0<sup>3,5</sup>]heptan - ein neues Valenzisomeres des Azepins
(1979)
No abstract available
No abstract available
No abstract available
No abstract available
No abstract available